NDC 53489-387 – Minoxidil
Minoxidil 10 mg/1 · Tablet · Oral
Product NDC53489-387
Product details
- Brand name
- Minoxidil
- Generic name
- minoxidil
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA072709
- Marketed since
- December 14, 1995
- Listing expires
- December 31, 2027
- Pharmacologic class
- Arteriolar Vasodilator
Active ingredients
- Minoxidil 10 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 53489-387-01 | 100 TABLET in 1 BOTTLE (53489-387-01) | Dec 14, 1995 |
| 53489-387-03 | 250 TABLET in 1 BOTTLE (53489-387-03) | Dec 14, 1995 |
| 53489-387-05 | 500 TABLET in 1 BOTTLE (53489-387-05) | Dec 14, 1995 |
| 53489-387-10 | 1000 TABLET in 1 BOTTLE (53489-387-10) | Dec 14, 1995 |
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